Canonical Allele Identifier: CA1677205982

Gene: PLG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741318G= , CM000668.2:g.160741318G=	GRCh38
NC_000006.11:g.161162350G= , CM000668.1:g.161162350G=	GRCh37
NC_000006.10:g.161082340G=	NCBI36
NG_016200.1:g.44126G= , LRG_571:g.44126G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.979G=	ENSP00000516619.1:p.Val327=
ENST00000418964.2:c.2077G=	ENSP00000389424.2:p.Val693=
ENST00000706906.1:c.*2046G=	ENSP00000516618.1:n.*2046G=
ENST00000308192.14:c.2026G= MANE Select	ENSP00000308938.9:p.Val676=
ENST00000308192.13:c.2026G=	ENSP00000308938.9:p.Val676=
ENST00000461414.2:n.49G=
ENST00000467466.1:n.327G=
NM_000301.3:c.2026G= , LRG_571t1:c.2026G=	NP_000292.1:p.Val676=
NM_000301.4:c.2026G=	NP_000292.1:p.Val676=
NM_000301.5:c.2026G= MANE Select	NP_000292.1:p.Val676=